rs72556287

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs72556287(C;C)

Make rs72556287(C;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

38401428

Gene

OTC

is a	snp
is	mentioned by
dbSNP	rs72556287
dbSNP (classic)	rs72556287
ClinGen	rs72556287
ebi	rs72556287
HLI	rs72556287
Exac	rs72556287
Gnomad	rs72556287
Varsome	rs72556287
LitVar	rs72556287
Map	rs72556287
PheGenI	rs72556287
Biobank	rs72556287
1000 genomes	rs72556287
hgdp	rs72556287
ensembl	rs72556287
geneview	rs72556287
scholar	rs72556287
google	rs72556287
pharmgkb	rs72556287
gwascentral	rs72556287
openSNP	rs72556287
23andMe	rs72556287
SNPshot	rs72556287
SNPdbe	rs72556287
MSV3d	rs72556287
GWAS Ctlg	rs72556287

Max Magnitude

0

ClinVar
Risk	rs72556287(C;C)
Alt	rs72556287(C;C)
Reference	Rs72556287(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	OTC
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.38260681G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000083483.1,